Disease #04380 (BBS9 (Bardet-Biedl syndrome, type 9), OMIM:615986)

Official abbreviation BBS9
Name Bardet-Biedl syndrome, type 9
OMIM ID 615986
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene BBS9
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2024-01-11 09:45:37 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00095115 - - - - ? - - - - Yes - BBS9 - - BBS9 2 1 Karen Stals
00276327 - - - F yes Turkey - 04y - - - BBS9 Obesity Rod cone dystrophy Polydactyly Renal abnormalities Genital abnormalities Behavioral problems Facial dysmorphism Cardiac abnormalities BBS9 BBS9 1 1 Evren Gümüş
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